(S)-3-Formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester is a chemical compound characterized by its isoquinoline structure, which features a fused bicyclic system. This compound contains a formyl group (-CHO) and a tert-butyl ester group, contributing to its reactivity and solubility properties. The presence of the carboxylic acid moiety indicates potential for hydrogen bonding and reactivity in various chemical transformations. The stereochemistry, denoted by the (S) configuration, suggests specific spatial arrangements that can influence its biological activity and interactions. This compound may exhibit properties typical of isoquinoline derivatives, such as potential pharmacological effects, making it of interest in medicinal chemistry. Its molecular structure allows for various functional group transformations, which can be exploited in synthetic organic chemistry. Additionally, the tert-butyl ester group enhances lipophilicity, potentially affecting its bioavailability and solubility in organic solvents. Overall, this compound represents a versatile scaffold for further chemical exploration and application in drug development.

(S)-3-FORMYL-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER

145525-27-5: (S)-3-Formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester is a chemical compound characterized by its isoquinoline structure, which features a fused bicyclic system. This compound contains a formyl group (-CHO) and a tert-butyl ester group, contributing to its reactivity and solubility properties. The presence of the carboxylic acid moiety indicates potential for hydrogen bonding and reactivity in various chemical transformations. The stereochemistry, denoted by the (S) configuration, suggests specific spatial arrangements that can influence its biological activity and interactions. This compound may exhibit properties typical of isoquinoline derivatives, such as potential pharmacological effects, making it of interest in medicinal chemistry. Its molecular structure allows for various functional group transformations, which can be exploited in synthetic organic chemistry. Additionally, the tert-butyl ester group enhances lipophilicity, potentially affecting its bioavailability and solubility in organic solvents. Overall, this compound represents a versatile scaffold for further chemical exploration and application in drug development.

CAS 145525-27-5

(S)-3-FORMYL-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER

2(1H)-Isoquinolinecarboxylic acid, 3-formyl-3,4-dihydro-, 1,1-dimethylethyl ester, (3S)-

Ref: IN-DA001D5M

3(S)-Formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Ref: 10-F735912